Reactive azo dyestuffs, free from anionic groups and containing a basic group and halogenotriazinyl radical and useful for dyeing cellulose/polyester

ABSTRACT

The invention is directed to reactive azo dyestuffs, free from anionic groups and which contain a basic group and a halogenotriazinyl radical and are of the general formula ##STR1## in which D is the radical of an organic azo dyestuff which is free from anionic groups and is preferably free from basic groups, 
     B is a direct bond or a bridge member to a ring C atom of D, 
     R 1  is H, alkyl, aralkyl or aryl and 
     W is a halogenotriazinyl radical containing a basic group; the dyestuffs are useful for the dyeing and printing of fibre materials containing cellulose.

This is a division, of application Ser. No. 760,212, filed 7/29/85 whichis continuation of Ser. No. 461,295 filed 1/27/83 (abandoned) which isdivision of 159,747 filed June 16, 1980 (now U.S. Pat. No. 4,503,224).

The present invention relates to reactive dyestuffs which are free fromanionic groups, in particular sulpho and carboxyl groups, and contain abasic group and a halogenotriazinyl radical.

Possible basic groups are, for example, primary, secondary or tertiaryamino groups, in particular alkylamino groups, or salts thereof, as wellas hydrazino and hydrazinium groups and quaternary ammonium groups.

The dyestuffs can contain one or more basic groups and one or morehalogenotriazinyl radicals, and can optionally contain other reactivegroups.

The basic group can be linked to the chromophore directly or via abridge member. It can also be, for example, a constituent of asubstituent on the triazine ring. Amino groups which are linked directlyto the triazine ring are not basic groups in the context of theinvention. Hydrazino or hydrazinium groups, however, are consideredbasic groups.

Preferred dyestuffs correspond to the following formulae ##STR2## inwhich D denotes the radical of an organic dyestuff which is free fromanionic groups and is preferably free from basic groups,

B denotes a direct bond or a bridge member to a ring C atom of D,

R₁ denotes H, alkyl, aralkyl or aryl and

W denotes a halogenotriazinyl radical containing a basic group,

wherein halogen denotes F, Cl or Br, and ##STR3## in which D₁ denotesthe radical of an organic dyestuff which is free from anionic groups andcontains a basic group and

W₁ denotes a halogenotriazinyl radical which is free from basic groups.

Examples of suitable basic groups which can be a constituent of D, D₁ orW are ##STR4## in which V denotes ##STR5## or a direct bond, B₁ denotesa bridge member, in particular C₂ -C₈ -alkylene, optionally interruptedby hetero-atoms, in particular --O--, aralkylene, alkarylene oralkarylalkylene, or, if ##STR6## also a direct bond, R₂, R₃, R₄ and R₅denote H or alkyl and R₂ and R₅ together can also denote alkylene,

An.sup.⊖ denotes an anion and

HX denotes an organic or inorganic acid.

Suitable radicals W₁ are those of the formula ##STR7## in which Udenotes the radical of an amine, alcohol or thiol or an alkyl, aryl oraralkyl radical, in particular ##STR8## in which R₆, R₇ and R₈ denote H,alkyl, aralkyl or aryl and

R₆ and R₇ together can also be a constituent of a 5-membered or6-membered ring.

Preferred radicals W are fluorotriazinyl radicals containing one radicalof the formula (III), (IIIa) or (IV), in particular those containing aradical ##STR9## in which B₂ denotes a direct bond, phenylene orphenylene--O-- and

alkylene denotes C₂ -C₈ -alkylene.

Anions An.sup.⊖ which are particularly suitable are those of highlyvolatile inorganic acids, such as hydrogen halide acids, or of organicacids, such as formic acid, acetic acid, propionic acid, chloroaceticacid, acrylic acid and oxalic acid.

The abovementioned acids are examples of suitable acids HX. Thefollowing are preferred: acetic acid, formic acid, propionic acid andhydrochloric acid.

Suitable dyestuffs are, for example, azo dyestuffs, anthraquinonedyestuffs, phthalocyanine dyestuffs, quinophthalone dyestuffs,phthaloperinone dyestuffs, nitro dyestuffs and formazan dyestuffs, inparticular those of the formula ##STR10## wherein A denotes the radicalof a diazo component and

K denotes the radical of a coupling component, in particular those ofthe formula ##STR11## in which R₉ denotes a substituent or H,

R₁₀ denotes H, NO₂, halogen, in particular Cl or Br, or CN and

K₁ denotes ##STR12## in which R₁₁ denotes alkyl, phenyl or cyclohexyl,

R₁₂ denotes H, alkyl, alkoxy or halogen, in particular Cl,

R₁₃ denotes H or sulphonamido, in particular ##STR13## in which R₁₄ andR₁₅ denote H, alkyl, aralkyl, aryl or a carboxylic acid ester group, inparticular --COOR₁₆,

in which

R₁₆ denotes alkyl or aralkyl, and

R₁₇ denotes H, alkyl, alkoxy or halogen, in particular Cl,

R₁₈ denotes H, alkyl or aryl,

R₁₉ denotes alkyl, in particular CH₃, carboxylic acid ester, inparticular --COO-alkyl, carboxamido, in particular ##STR14## or CN, R₂₀and R₂₁ denote H, alkyl or aralkyl,

R₂₂ denotes H, alkyl, aralkyl or aryl,

R₂₃ denotes H, alkoxy or R₁₉,

R₂₄ denotes H or alkyl,

R₂₅ denotes H, OH or alkyl, in particular CH₃,

Y denotes CN or carboxamido, in particular CONHR₂₆,

R₂₆ denotes H, alkyl or aryl,

R₂₇ denotes H or alkyl,

R₂₈ denotes OH or NH₂,

R₂₉ denotes alkyl or aryl,

R₃₀ denotes H or alkyl,

R₃₁ denotes alkyl or aralkyl,

R₃₂ denotes H, alkyl or --NHR₃₁ and

R₃₃ and R₃₄ denote H, alkyl or aryl.

Other particularly suitable dyestuffs are those of the formula ##STR15##wherein A denotes the radical of a diazo component,

R₃₅ denotes H, alkyl, alkoxy, halogen, in particular Cl, or acylamino,

R₃₆ denotes H, alkyl, alkoxy or halogen, in particular Cl, and

R₃₇ denotes H, alkyl or aralkyl, ##STR16## wherein R₃₈ denotes a bridgemember, in particular C₂ -C₆ -alkylene and especially --CH₂ --CH₂ --,and ##STR17## wherein R₃₉ denotes alkyl, in particular CH₃, carboxylicacid ester, in particular --COO-alkyl, or carboxamido, in particular##STR18## and R₄₀ denotes arylene or alkylene, in particular C₂ -C₆-alkylene.

Particularly suitable radicals A are the following: ##STR19## whereinR₄₁ denotes R₄₂ or acyl, in particular alkyl-, aralkyl- oraryl-carbonyl,

R₄₂ denotes H, CN, NO₂, alkyl, alkoxy, halogen, CF₃, alkyl-, aralkyl- oraryl-sulphonyl, carboxylic acid ester, in particular alkoxycarbonyl oraralkoxycarbonyl, or sulphonamido, in particular ##STR20## wherein R₄₃and R₄₄ denote H, alkyl, aralkyl or aryl, and

R₄₅ denotes H, CHO, SCN or alkoxy- or aralkoxycarbonyl,

R₄₆ denotes CN, alkoxycarbonyl or aralkoxycarbonyl,

R₄₇ denotes H or alkyl-, aralkyl-, or arylsulphonyl,

R₄₈ denotes alkyl, aryl, S-alkyl or S-aryl,

R₄₉ denotes H, alkyl, aryl or alkoxy- or aralkoxy-carbonyl,

R₅₀ denotes halogen, SCN, NO₂ or alkyl-, aralkyl- or aryl-sulphonyl,

R₅₁ denotes H or halogen,

R₅₂ denotes H, alkyl or alkoxy,

R₅₃ denotes H, alkyl, alkoxy, halogen, acylamino or alkoxy- oraralkoxy-carbonyl,

R₅₄ denotes H or alkyl and

R₅₅ denotes CN or alkoxy- or aralkoxy-carbonyl.

Further suitable dyestuffs are those of the formulae ##STR21## andanthraquinones of the formula ##STR22## wherein R₅₆ is preferably in the4- or 5-position and denotes H, NH₂, alkylcarbonylamino,arylcarbonylamino, alkylamino, cycloalkylamino, arylamino, OH, alkoxy,arylthio or nitro,

R₅₇ denotes H, alkoxy, aryloxy, nitro, halogen, cyano, alkylsulphonyl,arylsulphonyl, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl,alkoxysulphonyl, aralkoxysulphonyl or aryloxysulphonyl and

B₃ denotes a bridge member, preferably alkylene or arylene, ##STR23##wherein R₅₈ denotes NH₂ or OH and

R₅₉ denotes NH₂, alkylamino, cycloalkylamino, aralkylamino, arylamino,OH, alkylsulphonylamino, aralkylsulphonylamino, arylsulphonylamino,alkylcarbonylamino, aralkylcarbonylamino or arylcarbonylamino, and##STR24## wherein R₆₀, R₆₁ and R₆₂ denote H, OH, NH₂, alkylamino,arylamino or arylthio.

Preferred examples are those in which

R₆₁ and R₆₂ denote OH and

R₆₀ does not denote OH, or

R₆₀ and R₆₁ denote OH and

R₆₂ does not denote OH.

Quite generally, the alkyl, alkoxy, aryl and aralkyl radicals canoptionally contain further customary substituents. Preferred alkyl andalkoxy radicals contain 1-4C atoms, preferred aryl is optionallysubstituted phenyl and preferred arylene is optionally substitutedphenylene.

Dyestuffs which are generally preferred within the context of thoseclaimed, in particular within the context of the dyestuffs VIII-XX, arethose containing fluorotriazinyl radicals, especially those containingthe groups VI, VIa and VII.

Other suitable dyestuffs are those of the formulae VIII-XX which containW₁ instead of W and in which the group is on the chromophore.

The dyestuffs can be obtained by various processes:

(1) Reaction of dihalogenotriazinyl dyestuffs ##STR25## with compoundswhich contain a basic group and in addition a H atom which can reactwith halogen, in particular compounds of the formula ##STR26## in whichV₁ denotes ##STR27## it being possible, in the case where XXII or XXIIIis used, subsequently to carry out a quaternising step to introduce R₄and, in the case where XXII is used, to subject the product to saltformation with HX.

Examples of suitable compounds XXII-XXIV are:1-amino-2-dimethylaminoethane, 1-amino-2-diethylaminoethane,1-amino-2-N-methyl-N-propylaminoethane, 1-amino-2-dipropylaminoethane,1-amino-2-dibutylaminoethane, 1-amino-2-diisobutylaminoethane,1-methyl-2-dimethylaminoethane, 1-methylamino-2-diethylaminoethane,1-ethylamino-2-diethylaminoethane, 1-propylamino-2-diethylaminoethane,1-butylamino-2-diethylaminoethane, 1-methylamino-2-dibutylaminoethane,1-amino-2-bis-β-hydroxyethylaminoethane,1-amino-2-N-methyl-N-β-hydroxyethylaminoethane,1-β-hydroxyethylamino-2-diethylaminoethane,1-amino-3-dimethylaminopropane, 1-amino-3-diethylaminopropane,1-amino-3-dipropylaminopropane,1-amino-3-(N-methyl-N-β-hydroxyethylamino)-propane,1-amino-3-dibutylaminopropane, 1-methylamino-3-diethylaminopropane,1-methylamino-3-dipropylaminopropane,1-amino-3-N-methyl-N-isopropylaminopropane,1-amino-3-N-methyl-N-isobutylaminopropane,1-amino-3-diisobutylaminopropane, 2-amino-1-diethylaminopropane,1-amino-3-dimethylaminobutane, 1-dimethylamino-3-methylaminobutane,3-amino-1-diethylaminobutane, 1-amino-4-dimethylaminobutane,1-methylamino-4-dimethylaminobutane,1-amino-4-N-methyl-N-ethylaminobutane,1-methylamino-4-diethylaminobutane,1-amino-2-dimethylamino-2-methylpropane, 1-amino-5-dimethylaminopentane,1-amino-5-diethylaminopentane, 1-amino-6-diethylaminohexane,bis-(2-diethylamino-1-propyl)-amine, N-methylpiperazine,N-hydroxyethylpiperazine, N-(β-aminoethyl)-morpholine,N-methyl-N'-(β-aminoethyl)piperazine, 2-, 3- or4-aminobenzyl-dimethylamine, 2- or 4-(β-diethylaminoethoxy)-aniline, 2-or 4-(β-dimethylaminoethoxy)-aniline, 2-, 3- or4-amino-N,N-dimethylaniline, 1-amino-2-(2-dimethylaminoethoxy)-ethane,2-dimethylaminoethanol, 2-diethylaminoethanol,2-(2-dimethylaminoethoxy)-ethanol, 3-dimethylamino-1-propanol,1-dimethylamino-2-propanol, 1-diethylamino-2-propanol,1,3-bis-(dimethylamino)-2-propanol and 3- or4-dimethylaminomethylphenol.

Examples of suitable quaternising agents are: dimethyl sulphate, diethylsulphate, methyl toluenesulphate, ethyl toluenesulphate, methylchloride, methyl bromide and the like.

(2) Reaction of dyestuffs of the formula ##STR28## withhalogenotriazines of the formula

    halogen-W                                                  (XXVI)

which are in turn obtained from trihalogenotriazines and 1 mol of XXII,XXIII or XXIV.

(3) Reaction of dyestuffs of the formula ##STR29## with 1 mol percyanuric halide radical of a compound

    H-U                                                        (XXVIII)

(4) Reaction of dyestuffs of the formula ##STR30## with

    halogen-W.sub.1                                            (XXX)

XXX in turn being obtained from 1 mol of trihalogenotriazine and 1 molof a compound

    H-U TM (XXVIII)

Examples of suitable dyestuffs XXV and XXIX are: 1-amino-anthraquinone,1,4-diamino-anthraquinone, 1,5-diamino-anthraquinone,1,8-diamino-anthraquinone, 1-amino-4-benzoylamino-anthraquinone,1-amino-5-benzoylamino-anthraquinone,1-amino-5-acetylamino-anthraquinone,1-amino-8-benzoylamino-anthraquinone,1-amino-4-methylamino-anthraquinone, 1-amino-4-ethylamino-anthraquinone,1-amino-4-isopropylamino-anthraquinone,1-amino-4-cyclohexylamino-anthraquinone,1-amino-4-(4'-methylphenylamino)-anthraquinone,1-amino-4-(4'-methoxyphenylamino)-anthraquinone,1-amino-4-acetylamino-anthraquinone,1-amino-4-phenylamino-anthraquinone,1-amino-4-(3'-aminophenylamino)-anthraquinone,1-amino-4-(4'-aminophenylamino)-anthraquinone,1-(3'-aminophenylamino)anthraquinone,1-(4'-aminophenylamino)-anthraquinone,1-methylamino-4-(3'-aminophenylamino)-anthraquinone,1-methylamino-4-(4'-aminophenylamino)-anthraquinone,1-ethylamino-4-(3'-aminophenylamino)-anthraquinone,1-isopropylamino-4-(3'-aminophenylamino)-anthraquinone,1-isopropylamino-4-(4'-aminophenylamino)-anthraquinone,1-sec.-butylamino-4-(3'-aminophenylamino)-anthraquinone,1-n-butylamino-4-(4'-aminophenylamino)-anthraquinone,1-isobutylamino-4-(3'-aminophenylamino)-anthraquinone,1-isopropylamino-4-(4'-methylamino-anilino)-anthraquinone,1-methylamino-4-(3'-aminomethyl-4'-methylphenylamino)-anthraquinone,1-isopropylamino-4-(3'-methylaminomethyl-4'-methoxy-phenylamino)-anthraquinone,1-ethylamino-4-(4'-methylaminomethyl-phenylamino)-anthraquinone,1-cyclohexylamino-4-(3'-aminophenylamino)-anthraquinone,1-amino-4-hydroxy-anthraquinone, 1-amino-4-methoxy-anthraquinone,1-amino-4-(β-methoxyethoxy)-anthraquinone,1,4-diamino-2-phenoxy-anthraquinone,1,4-diamino-2-methoxy-anthraquinone,1,4-diamino-2-(β-methoxyethoxy)-anthraquinone,1,4-diamino-2-bromo-anthraquinone, 1,4-diamino-2-chloro-anthraquinone,1,4-diamino-2-methyl-anthraquinone, 1,4-diamino-2-nitroanthraquinone,1,4-diamino-2-cyano-anthraquinone, 1,4-diamino-2-acetyl-anthraquinone,1,4-diamino-2-formyl-anthraquinone,1,4-diamino-2-sulphophenoxy-anthraquinone,1,4-diamino-2-methylsulphonyl-anthraquinone,1,4-diamino-anthraquinone-2-carboxylic acid methyl ester,5-amino-thiazolanthrone, 1,4-diamino-2-(4'-aminophenoxy)-anthraquinone,1,4-diamino-2-(3'-aminophenoxy)-anthraquinone,1,4-diamino-2-sulpho-(3'-aminophenoxy)-anthraquinone,1,4-diamino-5-nitro-anthraquinone,1-amino-4-hydroxy-2-(4'-aminophenoxy)-anthraquinone,1-amino-4-hydroxy-2-(3'-aminophenoxy)-anthraquinone,1-amino-4-hydroxy-2-[β-(4'-aminophenoxy)-ethoxy]-anthraquinone,1-amino-4-hydroxy-2-[β-(phenylamino)-ethoxy]-anthraquinone,1-amino-4-hydroxy-2-(4'-aminomethylphenoxy)-anthraquinone,1-(4'-amino-phenylamino)-4-hydroxy-anthraquinone,1-(3'-amino-phenylamino)-4-hydroxy-anthraquinone,3,4-phthalo-2-amino-acridone, 1,5-diamino-4,8-dihydroxy-anthraquinone,1,8-diamino-4,5-dihydroxy-anthraquinone,1-amino-4,8-dihydroxy-5-(4'-methylphenylamino)-anthraquinone,1-amino-4,5-dihydroxy-8-(4'-methylphenylamino)-anthraquinone,1-amino-4,8-dihydroxy-5-phenylamino-anthraquinone,1-amino-4,5-dihydroxy-8-(4'-methoxyphenylamino)-anthraquinone,1-amino-4,8-dihydroxy-5-isopropylamino-anthraquinone,1-amino-4,5-dihydroxy-8-isopropylamino-anthraquinone,1-amino-4,8-dihydroxy-5-methylamino-anthraquinone,1-amino-4,5-dihydroxy-8-methylamino-anthraquinone,1-amino-5-methylamino-anthraquinone,1-amino-5-isopropylamino-anthraquinone,5-amino-1,4-bis-(4'-methylphenylamino)-anthraquinone,5-amino-1,4-bis-isopropylamino-anthraquinone,1-amino-4-chloro-5,8-bis-isopropylamino-anthraquinone,1-amino-4-chloro-5,8-bis-(4'-methylphenylamino)-anthraquinone,1-amino-5-methoxy-anthraquinone, 1-amino-8-methoxy-anthraquinone,1-amino-5-(β-methoxyethoxy)-anthraquinone,1-amino-5-nitro-anthraquinone, 1-amino-8-nitro-anthraquinone, an isomermixture of 1-amino-6- and -7-nitro-anthraquinone,1,4-diamino-anthraquinone-2,3-dicarboxylic acid 3'-aminophenylimide,1-(β-aminoethylamino)-4-(4'-methylphenylamino)-anthraquinone,1-amino-4-(3'-aminophenylamino)-2-methoxy-anthraquinone,1-amino-4-(4'-aminophenylamino)-2-phenoxy-anthraquinone,1-amino-4-(4'-methylaminomethyl-phenylamino)-2-phenoxy-anthraquinone,1-amino-2-methoxy-4-(4'-methylaminomethyl-phenylamino)-anthraquinone,5-amino-1,4-bis-phenylmercapto-anthraquinone,1-amino-4-(3-dimethylamino-1-propylamino)-anthraquinone,5-amino-1,4-bis-(3-dimethylamino-1-propylamino)-anthraquinone,1-amino-4-(4'-dimethylaminomethyl-phenylamino)-anthraquinone,1-amino-4-(3'-dimethylaminomethyl)-phenylamino)-anthraquinone,1-amino-4-(4'-diethylamino-methyl-phenylamino)-anthraquinone,1-amino-4-(4'-β-diethylaminoethoxy-phenylamino)-anthraquinone,1-amino-4-(2'-β-dimethylamino-ethoxy-phenylamino)-anthraquinone,5-amino-1,4-bis-(4'-β-diethylaminoethoxy-phenylamino)-anthraquinone,5-amino-1,4-bis-(4'-dimethylaminomethyl-phenylamino)-anthraquinone,5-amino-1,4-bis-(3'-dimethylaminomethylphenylamino)-anthraquinone,1-amino-4-(2'-dimethylaminomethyl-phenylamino)-anthraquinone,4'-amino-3-nitro-diphenylamine-1-sulphonic acid N,N-dimethylamide,4'-amino-3-nitro-diphenylamine-1-sulphonic acid N-methylamide,4'-amino-3-nitrodiphenylamine-1-sulphonic acid N-ethylamide,3'-amino-3-nitrodiphenylamine-1-sulphonic acid N-hydroxyethylamide,4'-amino-3-nitrodiphenylamine-1-sulphonic acid N-phenylamide,4'-amino-3-nitrodiphenylamine-1-sulphonic acid N-methylanilide,4'-amino-3-nitro-1-methylsulphonyldiphenylamine,4'-amino-3-nitro-1-ethylsulphonyldiphenylamine,3-nitro-diphenylamine-1-sulphonic acid N-(4"-amino-phenylamide),4'-methyl-3-nitrodiphenylamino-1-sulphonic acid N-(3"-aminophenylamide),4'-methoxy-3-nitrodiphenylamine-1-sulphonic acid N-(β-aminoethylamide),3-nitro-diphenylamine-1-sulphonic acid N-(β-aminoethylamide),3-nitro-4'-methoxy-diphenylamine-1-sulphonic acidN-(4"-aminophenylamide), 3-nitro-4'-methoxy-diphenylamine-1-sulphonicacid N-(3"-aminophenylamide),3-nitro-2'-methoxy-diphenylamine-1-sulphonic acidN-(4"-aminophenylamide),3-nitro-4'-acetylamino-diphenylamine-1-sulphonic acid(4"-aminophenylamide) and 3-nitro-4'-acetylamino-diphenylamine-1-sulphonic acid N-(β-aminoethylamide).

Examples of suitable compounds XXVIII are: ammonia, methylamine,dimethylamine, ethylamine, diethylamine, propylamine, isopropylamine,dipropylamine, butylamine, dibutylamine, methylethylamine, aminoethanol,diethanolamine, methylaminoethanol, morpholine, pyrrolidine, piperidine,cyclohexylamine, methylcyclohexylamine, benzylamine, benzylmethylamine,β-phenylethylamine, aniline and substituted anilines, such as 2-, 3- or4-methylaniline, 2-, 3- or 4-chloroaniline, 2-, 3- or 4-methoxyaniline,3- or 4-nitroaniline, 3- or 4-acetylaminoaniline,N-methyl-N-acetylaminoaniline, 2- or 4-β-hydroxyethoxyaniline, 2- or4-methylsulphonylaniline, 4-trifluoromethylaniline,3-(4-aminobenzenesulphonic acid dimethylamide, 3- or4-aminobenzenesulphonic acid methylamide, 2-, 3- or4-aminobenzenesulphonic acid methyl ester or ethyl ester,N-methylaniline and N-hydroxyethylaniline, phenol, 2-, 3- or4-methylphenol, 2-, 3-, or 4-chlorophenol, 2-, 3- or 4-ethylphenol,2,3-dimethylphenol, 3,4-, 2,4-, 3,5- or 2,5-dimethylphenol,2,3,5-trimethylphenol, 2-tert.-butylphenol, 4-tert.-butylphenol,4-(1,1-dimethyl-propyl)-phenol, 4-(1,1,3,3-tetramethylbutyl)-phenol,nonylphenol, dodecylphenol, 2-, 3- or 4-isopropylphenol, 2,4- or2,5-dichlorophenol, 2,4,5-trichlorophenol, 3- or 4-nitrophenol,3-chloro-4-nitrophenol, 4-chloro-2-methylphenol,5-chloro-2-methylphenol, 6-chloro-3-methyl-phenol,4-methyl-2-nitrophenol, 2-, 3- or 4-hydroxybenzoic acid methyl ester orethyl ester, 2-cyclohexylphenol, 4-cyclohexylphenol,2-cyclohexyl-4-methylphenol, 2-, 3- or 4-methoxyphenol, 2-(1-methylethoxy)-phenol, 2-ethoxyphenol, 2- or 4-phenoxyphenol, 2-, 3- or4-methylmercaptophenol, 3,5-dimethyl-4-(methylmercapto)-phenol, 2-, 3-or 4-hydroxybiphenyl, 2- or 4-benzylphenol,5,6,7,8-tetrahydro-1-naphthol, 1-naphthol, 2-naphthol,1-hydroxy-anthraquinone, 2-hydroxyanthraquinone, 2- or4-hydroxypyridine, 2- or 4-hydroxyquinoline,3-hydroxy-2-methylquinoline, methanol, ethanol, propanol, isopropanol,butanol, isobutanol, sec.-butanol, tert.-butanol, 2-methoxyethanol,2-ethoxyethanol, 2-chloroethanol, methylmercaptan, ethylmercaptan,mercaptoethanol and fluorophenol.

The condensation reactions can be carried out in organic solvents, suchas acetone, acetonitrile, benzene, toluene, xylenes, nitrobenzene,chlorinated hydrocarbons, dimethylformamide, formamide,N-methylpyrrolidone, tetramethylene sulphone, dioxane, tetrahydrofuraneand the like, in the presence of acid-binding organic bases, such as,for example, N,N-dimethylaniline, N,N-diethylaniline, trimethylamine,triethylamine, N,N-dimethylcyclohexylamine, diazabicyclooctane and thelike.

(5) Replacement of chlorine by fluorine in the triazine radical ofcorresponding chlorotriazinyl dyestuffs using alkali metal fluorides inorganic solvents, such as tetramethylene sulphone, N-methylpyrrolidoneand dimethylformamide.

(6) Coupling of diazotised amines with coupling components, the diazocomponent and/or the coupling component containing a halogenotriazinylradical and a basic group.

The new reactive dyestuffs, in the form of their salts or quaternarycompounds, are soluble in water and can be used, either individually oras mixtures, for dyeing and printing. They are suitable for use incontinuous dyeing and printing of synthetic fibre materials, such ascellulose esters, polyamide and, above all, polyester fibres, and forcontinuous dyeing and printing of cellulose fibres which can be swollenin water, and they are applied by the customary processes.

The process is particularly interesting for continuous dyeing andprinting of fibre blends of cellulose and synthetic fibres, inparticular cotton/polyester fibre blends, since it enables matchingshade dyeing or printing to be carried out by a one-stage procedure.Customary non-reactive disperse dyestuffs can optionally also be used.In this case, the process is preferably carried out in an acetic acidmedium. Known auxiliaries (dyestuff solvents or swelling agents), suchas are described, for example, in German Auslegeschrift No. 1,811,796and German Offenlegungsschriften Nos. 2,525,243, 2,528,743 and 2,751,830(preferably polyglycols), do not have to be used with the new type ofdyestuffs; however, the distribution of the dyestuff on thepolyester/cotton mixed fabric can be controlled by the addition ofrelatively small amounts (5-30 g/kg) of these auxiliaries.

Particularly good results are obtained if organic fixing auxiliaries(acid-trapping agents) are also used. Suitable fixing auxiliaries, whichare preferably used in amounts of 1-5 g/kg of padding liquor or printingpaste, are monoepoxides and polyepoxides, in particular the reactionproducts of aliphatic alcohols or polyols with epichlorohydrin. Exampleswhich may be mentioned are reaction products of alkylglycols, monoalkylethers of polyglycols or polyglycols, such as ##STR31## in which alkyldenotes C₁ -C₄ -alkyl and

alkylene denotes C₂ -C₄ -alkylene,

such as are described, for example, in German Patent Application P No.28 38 274.

It is preferable not to add an alkali in the dyeing and printingprocesses but to carry out the processes in a weakly acid medium.

On fibre blends, the new reactive dyestuffs produce dyeings and printsin colour shades which match well. The dyeings and prints aredistinguished by very good fastness properties, of which, in addition tofastness to sublimation, light and dry cleaning, fastness to wetprocessing should be singled out in particular.

Whilst in the abovementioned swelling process using selected dispersedyestuffs the dyestuffs can be completely extracted from the cellulosedyeings with, for example, N-methylpyrrolidone, the dyeings obtainedusing the new reactive dyestuffs are stable towards the extraction agentsince they have undergone covalent bonding to the cellulose fibre.

If they are not already in a water-soluble form, the new reactivedyestuffs are converted into such a form, preferably with organic acids,such as dilute acetic acid, before the dyeing or printing process. Thepadding liquor or printing paste can contain, in addition to water, thecustomary constituents such as dispersing agents, thickeners and/orswelling agents and/or dyestuff solubilising agents.

Dyeing is carried out by a procedure in which the textile materialscontaining cellulose fibres are impregnated with the aqueous paddingliquors in the customary manner, are squeezed off to a weight increaseof 40-100% and, if appropriate after intermediate drying for a shortperiod, are subjected to heat treatment at 190°-230° C. for 30-90seconds.

For printing, the printing pastes are prepared using the thickenerscustomary for reactive dyestuffs, such as alginates. The dyestuffs arefixed on the printed textile materials either by a dry heat treatment at180°-230° C. for one to two minutes or by a steam treatment at 170°-210°C. for two to fifteen minutes.

The dyestuffs are also suitable for dyeing pulp or paper from an aceticacid solution. Customary processes are used for dyeing paper, that is tosay either the pulp is first dyed, after adding sizing agents andaluminium sulphate, and sheets of paper are then produced, or finishedsheets of paper are dyed on the surface, after the addition of starch,by immersion in the dyeing solution.

EXAMPLE 1

11.0 g of 4'-amino-3-hydroxyquinophthalone are suspended in 60 ml ofnitrobenzene. 5.4 g of N,N-dimethylaniline are added to the suspension,and 6.0 g of 2,4,6-trifluorotriazine are added dropwise at 20° C. in thecourse of 10 minutes. After subsequently stirring the mixture for twohours, the condensation reaction has ended. 60 ml of toluene are allowedto run into the suspension and the precipitate is filtered off andwashed with toluene. The resulting filter cake is suspended in 80 ml oftoluene. 6.2 g of 1-amino-3-dimethylaminopropane are added dropwise tothe resulting suspension at 20° C. in the course of 30 minutes and themixture is subsequently stirred for 2 hours. The dyestuff suspension isfiltered and the filter cake is washed with toluene and dried in acirculating air cabinet at 60°.

A dyestuff of the formula ##STR32## which is readily soluble in diluteacetic acid is obtained. From this solution, the dyestuff producesmatching shade yellow dyeings with very good fastness to wet processingand rubbing and excellent fastness to light or polyester/cotton fibreblends by the processes of Examples 2 and 3.

A very similar dyestuff is obtained if, instead of4'-amino-3-hydroxyquinophthalone an equivalent amount of a mixture of3'- and 4'-amino-3-hydroxyquinophthalone is used.

EXAMPLE 2

10.5 g of the dyestuff obtained according to Example 1 are suspended inwater and are dissolved by pouring 30 ml of 30% strength acetic acidover the suspension. The solution formed is made up to 1,000 ml. Apolyester/cotton mixed fabric with a polyester/cotton ratio of 65/35 isimpregnated with the aid of a padder, the liquor pick-up of the fabricbeing about 65%. The fabric treated in this manner is dried and thedyestuff is fixed on the two fibres by a hot air treatment in athermosol unit at 215° for 60 seconds. After customary after-treatmentby soaping close to the boiling point and after drying, a completelyneutral yellow shade which matches well on the two fibre materials isobtained. The finished dyeing exhibits good fastness to daylight, goodfastness to rubbing when dry or wet and outstanding fastness to wetprocessing.

Instead of the hot air treatment described, the padded polyester/cottonmixed fabric can also be subjected to a steaming process at 175° C. for8 minutes.

EXAMPLE 3

10.5 g of the dyestuff obtained according to Example 1 are suspended inwater and are dissolved with 30 ml of 30% strength dilute acetic acid.4.0 g of an epoxide compound of the formula ##STR33## 26.0 g of apolyethylene glycol ether of molecular weight 400 and 10.0 g of a 10%strength aqueous solution of a customary thickener are added and theentire mixture is made up to 1,000 ml with water.

A polyester/cotton mixed fabric is dyed, as described in Example 2,using the padding liquor prepared in this manner.

In a modification of the procedure described, instead of using diluteacetic acid, the dyestuff can also be dissolved by being suspended inwater and adjusting the pH value to 3.5-4 by carefully adding 10%strength hydrochloric acid.

EXAMPLE 4

11.2 g of 1-amino-anthraquinone are suspended or dissolved in 100 ml ofnitrobenzene and 12.5 ml of dimethylformamide. 7.3 g of2,4,6-trifluorotriazine are added dropwise in the course of 30 minutes,the mixture is subsequently stirred for 30 minutes and the temperatureis then increased to 50°. The mixture is subsequently stirred at thistemperature for 30 minutes, cooled to 20° and diluted with 125 ml ofmethanol, and the difluorotriazinylaminoanthraquinone is filtered off,and dried at 50° in a circulating air drying cabinet.

15.8 g of the resulting intermediate product are suspended in 90 ml oftoluene. 9.5 g of 1-amino-3-dimethylaminopropane are added dropwise inthe course of 30 minutes and the mixture is subsequently stirred for afurther hour. The dyestuff which has precipitated is filtered off,washed with toluene and ligroin and dried at 50° in a circulating aircabinet. It has the formula ##STR34## and dyes polyester/cottonmixtures, from a weakly acid solution by the process of Examples 2 and3, in uniform yellow shades which are fast to light, rubbing and wetprocessing.

EXAMPLE 5

10.3 g of 1-amino-4,8-dihydroxy-5-isopropylamino-anthraquinone areintroduced into 80 ml of nitrobenzene and 20 ml of dimethylformamide.4.8 g of 2,4,6-trifluorotriazine are added dropwise in the course of 5minutes, during which the temperature is allowed to rise to 30°. Themixture is then kept at 30°-35° for 15 minutes, the temperature issubsequently further increased to 50° and the mixture is then stirred atthis temperature for 15 minutes. It is cooled to 20° and diluted with100 ml of methanol. The intermediate product which has precipitated isfiltered off, washed with methanol and dried at 50° in a circulating aircabinet.

8.5 g of the resulting product are stirred in 85 ml of toluene. 4.1 g of1-amino-3-dimethylaminopropane are added dropwise to the suspension inthe course of 15 minutes, during which the temperature is allowed torise to 35°. After 30 minutes at 65°, the reaction has ended. Theresulting dyestuff of the formula ##STR35## is filtered off, washed withtoluene and petroleum ether and dried at 60° in a circulating aircabinet.

On polyester/cotton mixtures, the dyestuff produces, by the process ofExample 3, uniform blue dyeings which are fast to light, wet processingand rubbing.

EXAMPLE 6

15 g of 1-amino-2-(4'-aminophenoxy)-4-hydroxyanthraquinone are suspendedin 45 ml of nitrobenzene and 6.3 g of N,N-dimethylaniline. 7.1 g of2,4,6-trifluorotriazine are added dropwise at 20° in the course of 10minutes and, after subsequently stirring the mixture for one hour, afterwhich the condensation reaction has ended, the dyestuff which hasprecipitated is filtered off, washed with methanol and dried at 50° in acirculating air cabinet.

16.5 g of the resulting difluorotriazinylamino dyestuff are suspended in90 ml of toluene. 6.7 g of 1-amino-3-dimethylamino-propane are addeddropwise in the course of 45 minutes, starting at 20°, the temperaturegradually rising to 30°. After subsequently stirring the mixture for onehour, the condensation reaction has ended. The dyestuff of the formula##STR36## which is present in the form of a suspension, is filtered off,washed with toluene and dried at 60° in a circulating air cabinet. Thedyestuff, which is soluble in dilute acetic acid, dyes polyester/cottonmixed fabric in solid red shades with very good fastness properties bythe processes of Examples 2 and 3.

EXAMPLE 7

6.0 g of 2,4,6-trifluorotriazine are added dropwise to 16 g of1-amino-4-hydroxy-2-(β-N-phenylaminoethoxy)-anthraquinone in 65 ml ofnitrobenzene and 5.4 g of N,N-dimethylaniline at 10° in the course of 15minutes. The temperature is then allowed to rise gradually to 20° andthe mixture is subsequently stirred for about 2 hours in total. When thereaction has ended, the difluorotriazinyl intermediate product isfurther precipitated by adding 65 ml of isopropanol and is filtered offand the filter cake is washed with isopropanol and dried at 60° in acirculating air cabinet.

21.2 g of the resulting product are suspended in 100 ml of toluene. 8.8g of 1-amino-3-dimethylaminopropane are added dropwise at 20°-25° in thecourse of 30 minutes and the condensation reaction is brought tocompletion in the course of one hour. The dyestuff precipitate isfiltered off and the cake is washed with toluene and dried at 60° in acirculating air cabinet. The resulting dyestuff corresponds to theformula ##STR37## and dyes mixtures of polyester/cotton, from an aceticacid solution, according to Example 2, in uniform red shades withexcellent fastness properties.

EXAMPLE 8

24 g of 5-amino-1,4-bis-phenylthio-anthraquinone are suspended in 80 mlof nitrobenzene and 8.3 g of N,N-dimethylaniline. 9.2 g of2,4,6-trifluorotriazine are added dropwise at 20° in the course of 15minutes and the mixture is subsequently stirred for 1 hour in order tobring the condensation reaction to completion. The precipitate isfiltered off and the filter cake is washed with methanol and dried at50° in a circulating air cabinet.

20.5 g of the resulting condensation product are suspended in 100 ml oftoluene. 7.8 g of 1-amino-3-dimethylaminopropane are added dropwise at20°-25° in the course of 1 hour and the mixture is then subsequentlystirred for a further 2 hours. The dyestuff which has precipitated isnow filtered off, washed with toluene and dried at 60° in a circulatingair cabinet. It corresponds to the formula ##STR38## and uniformly dyespolyester/cotton fibre blends, from dilute acetic acid solutions by theprocess of Examples 2 and 3, in scarlet-red shades with very goodfastness to wet processing.

EXAMPLE 9

12 g of 1-amino-4-hydroxy-anthraquinone are suspended in 60 ml ofnitrobenzene and 25 ml of dimethylformamide. 7.5 g of2,4,6-trifluorotriazine are then added dropwise in the course of 5minutes, during which the temperature rises to 40°. The reaction mixtureis warmed further to 50°-55° for 30 minutes, until the condensationreaction has ended. The mixture is allowed to cool and is diluted with100 ml of methanol and the product is filtered off and washed withmethanol. The difluorotriazinylamino-hydroxyanthraquinone obtained isdried in a circulating air cabinet at 60°.

8.5 g of the resulting intermediate product are stirred in 80 ml oftoluene. 5.8 g of 1-amino-2-diethylaminoethane are added dropwise in thecourse of 15 minutes, during which the temperature is allowed to rise to35°. After subsequently stirring the mixture for 30 minutes, thecondensation reaction has ended. The dyestuff which has precipitated isfiltered off at 20°, washed with toluene and petroleum ether and driedat 50° in a circulating air cabinet. The resulting dyestuff correspondsto the formula ##STR39## and, after being dissolved in dilute aceticacid, produces solid scarlet-red dyeings, with good fastness to light,rubbing and wet processing, on polyester/cotton mixtures by theprocesses of Examples 2 and 3.

EXAMPLE 10

13.1 g of 1,4-diamino-anthraquinone-2-sulphonic acid phenyl ester areintroduced into 90 ml of nitrobenzene and 20 ml of dimethylformamide.4.8 g of 2,4,6-trifluorotriazine are added dropwise in the course of 5minutes and the mixture is subsequently stirred at 30°-40° for 30minutes and at 50°-55° for 30 minutes. It is diluted, at 20°, with 120ml of methanol. The product which has precipitated is filtered off,washed with methanol and dried at 50° in a circulating air cabinet. 10.2g of the resulting product are stirred in 80 ml of toluene. 4.1 g of1-amino-3-dimethylaminopropane are added dropwise to the suspension inthe course of half an hour. The mixture is subsequently stirred at25°-30° for 30 minutes, until a sample examined by chromatographyindicates that the condensation reaction has ended. The resultingprecipitate is filtered off and the filter cake is washed with tolueneand petroleum ether and dried at 50° in a circulating air cabinet. Theresulting dyestuff corresponds to the formula ##STR40## After beingdissolved in a weakly acid medium, this dyestuff uniformly dyespolyester/cotton mixtures, by the processes of Examples 2 and 3, inviolet shades which are fast to light, wet processing and rubbing.

EXAMPLE 11

11.0 g of 1,4-diamino-2-phenoxy-anthraquinone are introduced into 70 mlof nitrobenzene and 20 ml of dimethylformamide. 4.8 g of2,4,6-trifluorotriazine are added dropwise in the course of 5 minutesand the mixture is then warmed to 30°-35° for 30 minutes and thereafterto 50°-55° for 30 minutes. When the condensation reaction has ended, themixture is diluted with 120 ml of methanol. The intermediate productwhich has crystallised out is filtered off, washed with methanol anddried at 60° in a circulating air cabinet.

8.9 g of the resulting difluorotriazinylamino compound are suspended in70 ml of toluene. 4.1 g of 1-amino-3-dimethyl-aminopropane are addeddropwise in the course of 15 minutes, during which the temperature isallowed to rise to about 30°-35°. The mixture is subsequently stirredfor a further 30 minutes and the dyestuff which has precipitated is thenfiltered off, washed with toluene and then with petroleum ether anddried in a circulating air cabinet. The dyestuff of the formula##STR41## produces uniform dyeings, which are fast to light, wetprocessing and rubbing, in a violet colour shade on polyester/cottonmixtures from an acetic acid dyeing solution by the processes describedin Examples 2 and 3.

EXAMPLE 12

10.2 g of the 1-(4,6-difluoro-2-triazinylamino)anthraquinone obtainedaccording to Example 4 are stirred in 50 ml of toluene. 9.5 g of4-amino-1-diethylaminopentane are added dropwise in the course of 30minutes. The mixture is subsequently stirred for several hours in orderto bring the condensation reaction to completion. Thereafter, it ispoured slowly into 150 ml of petroleum ether, which has been cooled to5°-10°, and the mixture is subsequently stirred at this temperature forsome time, the precipitate is then filtered off and the filter cake iswashed with petroleum ether. After drying at 50° in a circulating aircabinet, a product is obtained which corresponds to the formula##STR42## and dyes polyester/cotton mixtures, from a weakly acidsolution by the processes of Examples 2 and 3, in solid yellow shadeswhich are fast to light, wet processing and rubbing.

EXAMPLE 13

10.2 g of the 1-(4,6-difluoro-2-triazinylamino)-anthraquinone preparedaccording to Example 4 are stirred in 100 ml of toluene. 3.0 g oftriethylamine and 4.5 g of 2-diethylaminoethanol are added and themixture is heated to 60°-65° for 3 hours and thereafter to 80°-85° for afurther hour. It is then cooled to 20°. 170 ml of petroleum ether areadded to the reaction mixture and the dyestuff which has precipitated isfiltered off, washed with petroleum ether and dried at 60° in acirculating air cabinet. The dyestuff of the formula ##STR43## producessolid dyeings, which are very fast to wet processing and rubbing, onpolyester/cotton mixtures from an acetic acid solution by the processesof Examples 2 and 3.

EXAMPLE 14

If the 4.1 g of 1-amino-3-dimethylaminopropane in Example 5 are replacedby 5.2 g of 1-amino-3-(N-methyl-N-hydroxyethylamino)-propane and theprocedure is otherwise as described in that example, a dyestuff of theformula ##STR44## which has coloristic properties very similar to thoseof the dyestuff described in Example 5, is obtained.

EXAMPLE 15

18 g of the dyestuff of Example 6 are dissolved in 120 ml ofnitrobenzene. After warming the solution to 60°, 4.5 g of dimethylsulphate are added dropwise in the course of 10 minutes. After 30minutes, a chromatogram of a sample shows that the reaction has ended.The resulting dyestuff suspension is cooled to 20° and the dyestuff isfiltered off, covered twice with nitrobenzene and then washed withtoluene.

After drying at 50° in a circulating air cabinet, a dyestuff of theformula ##STR45## which uniformly dyes polyester/cotton mixtures in redshades with excellent fastness properties by the processes of Examples 2and 3 is obtained.

EXAMPLE 16

11.2 g of the 1-(4,6-difluoro-2-triazinylamino)anthraquinone preparedaccording to Example 4 are suspended in 50 ml of nitrobenzene. 5.0 g of2-aminobenzyl-N,N-dimethylamine are added to the suspension and stirringis continued for 11/2 hours at 20°-30°, during which increasingly moresolid dissolves. When the condensation reaction has ended, 120 ml ofpetroleum ether are added, the mixture is subsequently stirred for 1hour in order to bring the precipitation to completion and the dyestuffwhich has precipitated is filtered off and washed with petroleum ether.After drying at 60° in a circulating air cabinet, a dyestuff is obtainedwhich is readily soluble in dilute acetic acid, has the formula##STR46## and uniformly dyes polyester/cotton mixtures in yellow shades,which are fast to light, wet processing and rubbing, by the processes ofExamples 2 and 3.

A similar dyestuff is obtained if, instead of2-aminobenzyl-N,N-dimethylamine, 5.0 g of4-aminobenzyl-N,N-dimethylamine are employed.

EXAMPLE 17

8.0 g of 1-amino-4-hydroxy-2-(β-N-phenylaminoethoxy)-anthraquinone aresuspended in 40 ml of nitrobenzene and 2.7 g of N,N-dimethylaniline. 3.0g of 2,4,6-trifluorotriazine are added dropwise at 10° in the course of15 minutes and the temperature is then allowed to rise gradually to 20°.The product which has precipitated is filtered off, washed with methanoland dried at 50° in a circulating air cabinet.

8.0 g of the resulting intermediate product are suspended or dissolvedin 50 ml of dimethylformamide. A solution of 7.3 g of4-(β-diethylaminoethoxy)-aniline in 15 ml of methanol is added dropwisein the course of 30 minutes. Fine needles are formed, and theirprecipitation is increased, when the reaction has ended, by adding afurther 250 ml of methanol. The precipitate is filtered off, washed withmethanol and dried at 50° in a circulating air cabinet. The resultingdyestuff corresponds to the formula ##STR47## and uniformly dyespolyester/cotton mixtures in red shades with good fastness properties bythe processes of Examples 2 and 3.

Further anthraquinone dyestuffs which are summarised in Table I andwhich give, after being dissolved in a weakly acid medium, solid fastdyeings of the shades indicated on polyester/cotton mixtures by theprocesses of Examples 2 and 3 can be prepared in an analogous manner.

                                      TABLE I    __________________________________________________________________________    Example                                                  Colour    No.  Dyestuff                                            shade    __________________________________________________________________________    18          ##STR48##                                          yellow    19          ##STR49##                                          yellow    20          ##STR50##                                          blue    21          ##STR51##                                          violet    22          ##STR52##                                          blue    23          ##STR53##                                          blue    24          ##STR54##                                          blue    25          ##STR55##                                          orange    26          ##STR56##                                          green    27          ##STR57##                                          blue    28          ##STR58##                                          red    29          ##STR59##                                          scarlet    30          ##STR60##                                          red    31          ##STR61##                                          blue    32          ##STR62##                                          red    33          ##STR63##                                          orange    34          ##STR64##                                          blue    35          ##STR65##                                          blue    36          ##STR66##                                          blue    37          ##STR67##                                          blue    38          ##STR68##                                          violet    39          ##STR69##                                          blue    40          ##STR70##                                          red    41          ##STR71##                                          blue-violet    42          ##STR72##                                          blue    43          ##STR73##                                          blue    44          ##STR74##                                          blue    45          ##STR75##                                          violet    46          ##STR76##                                          violet    47          ##STR77##                                          scarlet    48          ##STR78##                                          blue    49          ##STR79##                                          red    50          ##STR80##                                          blue    51          ##STR81##                                          violet    52          ##STR82##                                          blue    53          ##STR83##                                          blue-green    54          ##STR84##                                          blue    55          ##STR85##                                          blue    56          ##STR86##                                          blue    57          ##STR87##                                          blue    58          ##STR88##                                          green    59          ##STR89##                                          yellow    60          ##STR90##                                          blue    61          ##STR91##                                          yellow    62          ##STR92##                                          red-violet    63          ##STR93##                                          red    64          ##STR94##                                          blue    65          ##STR95##                                          blue    66          ##STR96##                                          yellow    67          ##STR97##                                          red    68          ##STR98##                                          blue    69          ##STR99##                                          yellow    70          ##STR100##                                         yellow    71          ##STR101##                                         yellow    72          ##STR102##                                         blue    73          ##STR103##                                         blue    __________________________________________________________________________

EXAMPLE 74

16 g of 4-amino-2'-hydroxy-5'-methylazobenzene are suspended in 80 ml oftoluene and 9.8 g of N,N-dimethylaniline. 10.4 g of2,4,6-trifluorotriazine is added dropwise to the suspension at 20° andthe mixture is subsequently stirred for a further 45 minutes. When thecondendation reaction has ended, 14.4 g of1-amino-3-dimethylaminopropane are added dropwise at 20°-25° in thecourse of 30 minutes. The resulting suspension is subsequently stirredfor 2 hours and the dye-stuff which has precipitated is filtered off,washed with toluene and dried at 60° in a circulating air cabinet. Theproduct corresponds to the formula ##STR104## and gives, onpolyester/cotton mixtures from acetic acid solution by the processes ofExamples 2 and 3, solid, strong yellow dyeings with excellent fastnessto light and very good fastness to wet processing and rubbing.

EXAMPLE 75

12 g of 4-amino-4'-methoxy-2-methylazobenzene are introduced into 50 mlof nitrobenzene and 20 ml of dimethylformamide. 7.5 g of2,4,6-trifluorotriazine are added dropwise to the mixture in the courseof 20 minutes and the mixture is subsequently stirred at 25°-30° for 1hour. The resulting well-formed crystals of thedifluorotriazinylaminoazo dyestuff are filtered off, covered twice withnitrobenzene, washed with petroleum ether and dried at 50° in acirculating air cabinet. 7.2 g of the resulting intermediate product aresuspended in 60 ml of toluene. 4.1 g of 1-amino-3-dimethylaminopropaneare added dropwise at 25°-30° in the course of 30 minutes and themixture is subsequently stirred for 30 minutes. The resulting dyestuffof the formula ##STR105## is filtered off, washed with a little tolueneand then with petroleum ether and dried at 50° in a circulating aircabinet.

The dyestuff gives, on polyester/cotton fibre blends from a weakly acidsolution by the processes of Examples 2 and 3, solid yellow dyeingswhich are very fast to light, wet processing and rubbing.

EXAMPLE 76

14 g of 1-(4'-amino-2'-nitrophenylazo)-2-hydroxynaphthalene aresuspended in 120 ml of nitrobenzene and 5.8 g of N,N-dimethylaniline.6.3 g of 2,4,6-trifluorotriazine are added dropwise at 20° in the courseof 10 minutes. After subsequently stirring the mixture for one houruntil the reaction has ended, 8.2 g of 1-amino-3-dimethylaminopropaneare then added dropwise at 20°-25° in the course of 30 minutes and themixture is subsequently stirred for 2-3hours. During the dropwiseaddition of the amine component and the subsequent stirring, the colourof the suspension changes from a brownish to a clear lighter red shade.The dyestuff which has precipitated is filtered off, washed with tolueneand petroleum ether and dried at 50° in a circulating air cabinet. Thedyestuff of the formula ##STR106## uniformly dyes polyester/cottonmixtures, from an acetic acid solution by the processes of Examples 2and 3, in red shades with very good fastness properties.

Further azo dyestuffs, listed in Table II, which produce uniform dyeingsand prints, which are fast to washing and have the shades indicated, onpolyester/cotton fibre blends by the procedure of Examples 2 and 3 canbe prepared analogously to the above examples.

                                      TABLE II    __________________________________________________________________________    Ex-    am-    ple                                                        Colour    No.       Dyestuff                                                shade    __________________________________________________________________________    77        ##STR107##                                             orange    78        ##STR108##                                             yellow    79        ##STR109##                                             orange    80        ##STR110##                                             orange    81        ##STR111##                                             yellow    82        ##STR112##                                             orange    83        ##STR113##                                             yellow    84        ##STR114##                                             yellow    85        ##STR115##                                             yellow    86        ##STR116##                                             brown    87        ##STR117##                                             yellow    88        ##STR118##                                             yellow    89        ##STR119##                                             yellow    90        ##STR120##                                             yellow    91        ##STR121##                                             yellow    92        ##STR122##                                             yellow    93        ##STR123##                                             yellow    94        ##STR124##                                             orange    95        ##STR125##                                             red    96        ##STR126##                                             violet    97        ##STR127##                                             red    98        ##STR128##                                             yellow    99        ##STR129##                                             yellow    100        ##STR130##                                             yellow    101        ##STR131##                                             yellow    102        ##STR132##                                             orange    103        ##STR133##                                             yellow    104        ##STR134##                                             yellow    __________________________________________________________________________

EXAMPLE 105

A solution of 12.2 g of 3-amino-N,N-dimethylaniline in 40 ml of acetoneis added dropwise to a solution of 12.9 g of 2,4,6-trifluorotriazine in40 ml of acetone at -5° to 0° in the course of 30 minutes. Thesuspension of crystals is subsequently stirred for 15 minutes, afterwhich the condensation reaction has ended. 19.5 g of1-amino-3-dimethylaminopropane are now added dropwise at 20° in thecourse of 45 minutes and the mixture is subsequently stirred for afurther hour, until a chromatogram no longer indicates the presence ofthe difluoroarylaminotriazine. The resulting solution is poured into 500ml of ice-water and the pH value is adjusted to 4.5 by carefully addinghydrochloric acid. A suspension of a diazonium salt which has beenobtained by diazotising 12.4 g of 4-nitroaniline in 200 ml of water and30 ml of concentrated hydrochloric acid with 6.2 g of sodium nitrite in100 ml of water is added to the resulting solution. During the additionof the diazonium salt, the pH value of the coupling mixture is kept at4.5-5.5 with sodium carbonate solution. After subsequently stirring themixture for two hours, the temperature is allowed to rise gradually to20° and the pH value is kept at 6.0-6.5. Finally, the pH is adjusted to7, 70 g of sodium chloride are also added to the suspension and thedyestuff is filtered off and washed with dilute sodium chloridesolution. The resulting dyestuff corresponds to the formula ##STR135##

It dyes polyester/cotton mixed fabric, from acetic acid solution by theprocesses of Examples 2 and 3, in uniform, red colour shades which arefast to wet processing. III and give, on polyester/cotton fibre blendsby the methods of Examples 2 and 3, solid dyeings which are fast towashing and have the shades indicated can be prepared by an analogousprocedure.

                                      TABLE III    __________________________________________________________________________    Example No.           Dyestuff                                   Colour    __________________________________________________________________________                                                      shade    106            ##STR136##                                red    107            ##STR137##                                violet    108            ##STR138##                                red    109            ##STR139##                                red    110            ##STR140##                                orange-red    __________________________________________________________________________

EXAMPLE 111 14 g of 4'-amino-3-nitro-diphenylamine-1-sulphonic acidN,N-dimethylamide are dissolved in 60 ml of dimethylformamide. Aftercooling the solution to 0°-5°, 6.3 g of 2,4,6-trifluorotriazine areadded dropwise in the course of 5 minutes and the mixture issubsequently stirred for a further 30 minutes until the condensationreaction has ended. 8.6 g of 1-amino-3-dimethylaminopropane are addeddropwise at 0°-5° in the course of 30 minutes. The temperature is thenallowed to rise to 20°. After subsequently stirring the mixture for halfan hour, the reaction has ended. The resulting solution is now addeddropwise to 1,500 ml of 10% strength sodium chloride solution at 0°-5°.The precipitate formed is filtered off, stirred again with cold 10%strength sodium chloride solution, filtered off again, rinsed with alittle cold 10% strength sodium chloride solution and dried at 60° in acirculating air cabinet. The resulting dyestuff corresponds to theformula ##STR141## and dyes polyester/cotton mixtures in uniform yellowshades with good fastness properties from an acetic acid solution by theprocesses of Examples 2 and 3.

In the same manner, solid yellow dyeings and prints can be produced onpolyester/cotton mixtures by the processes indicated in Examples 2 and 3using the analogously prepared nitro dyestuffs listed in Table IV.

                                      TABLE IV    __________________________________________________________________________    Exam-    ple No.        Dyestuff    __________________________________________________________________________    112         ##STR142##    113         ##STR143##    114         ##STR144##    115         ##STR145##    116         ##STR146##    117         ##STR147##    118         ##STR148##    __________________________________________________________________________

EXAMPLE 119 33.5 g of 1-amino-anthraquinone, 330 ml of nitrobenzene and41.6 g of cyanuric chloride are heated to 90°. After 1 hour, thetemperature is increased to 120° and the mixture is stirred at thistemperature for 30 minutes to 1 hour until the condensation reaction hasended. The suspension is cooled to 30° and the yellow crystals arefiltered off, washed with methanol and dried at 50° C. in a circulatingair cabinet.

11.2 g of 1-(4,6-dichloro-2-triazinylamino)anthraquinone are suspendedin 120 ml of toluene. 6.1 g of 1-amino-3-dimethylaminopropane are addeddropwise at 25°-30°, this temperature is maintained for 30 minutes andthe mixture is then heated to 55°-60° for a further hour. It issubsequently allowed to cool and the dyestuff which has precipitated isfiltered off and washed twice with a little toluene and then withpetroleum ether. The product is dried at 50° in a circulating aircabinet. It corresponds to the formula ##STR149## and uniformly dyespolyester/cotton mixed fabric in yellow shades from an acetic acidsolution by the processes of Examples 2 and 3.

EXAMPLE 120 11.2 g of 1-(4,6-dichloro-2triazinylamino)anthraquinone aresuspended in 120 ml of toluene.

7.2 g of 2-diethylaminoethanol and 3.1 g of triethylamine are added, themixture is heated to 60°-65°, a further 3.0 g of triethylamine aresubsequently added after 7 hours and the temperature is kept at 60°-65°for a further 5 hours. When the condensation reaction has ended, themixture is cooled, the precipitate is filtered off and the filter cakeis washed with a little toluene and then with ligroin and dried at 60°in a circulating air cabinet. After dissolving the resulting dyestuff ofthe formula ##STR150## in dilute acetic acid, solid yellow dyeings whichare fast to light, wet processing and rubbing are produced onpolyester/cotton mixtures by the process of Example 3.

Further dyestuffs, summarised in Table V, which produce solid dyeings inthe colour shades indicated on polyester/cotton mixtures by the dyeingprocesses of Examples 2 and 3 can be synthesised in an analogous manner.

                                      TABLE V    __________________________________________________________________________    Ex-    am-    ple                                                      Colour    No.       Dyestuff                                              shade    __________________________________________________________________________    121        ##STR151##                                           yellow    122        ##STR152##                                           yellow    123        ##STR153##                                           yellow    124        ##STR154##                                           yellow    125        ##STR155##                                           yellow    126        ##STR156##                                           scarlet    127        ##STR157##                                           red    128        ##STR158##                                           red-violet    129        ##STR159##                                           blue    130        ##STR160##                                           blue    __________________________________________________________________________

EXAMPLE 131 10 g of the intermediate product of the formula ##STR161##prepared according to Example 6, are suspended in 100 ml of toluene.

2.8 g of 1,4-diaminobutane are added dropwise at 5°-10° in the course of30 minutes and the mixture is subsequently stirred for 1 hour. Theprecipitate is filtered off and washed with toluene and then withpetroleum ether. After drying at 50° in a circulating air cabinet, adyestuff is obtained which essentially corresponds to the formula##STR162## and produces uniform red dyeings, which are fast to wetprocessing, on polyester/cotton mixed fabric from an acetic acidsolution by the processes of Examples 2 and 3.

A similar dyestuff is obtained if 1.8 g of 1,2-diaminoethane areemployed instead of the 1,4-diaminobutane.

EXAMPLE 132

16 g of 1-amino-4-(3'-amino-phenylamino)-2-bromoanthraquinone aresuspended in 80 ml of toluene and 5.4 g of N,N-dimethylaniline. 6.0 g of2,4,6-trifluorotriazine are added dropwise at 20° in the course of 10minutes and the mixture is subsequently stirred for a further 45minutes. The dyestuff intermediate product has precipitated completely.8.3 g of 1-amino-3-dimethyl-aminopropane are added dropwise to thesuspension at 20°-25° in the course of 30 minutes and the mixture issubsequently stirred for 2 hours in order to bring the condensationreaction to completion. The suspended dyestuff is filtered off, washedwith a little toluene and then with petroleum ether and dried at 60° ina circulating air cabinet. The resulting dyestuff of the formula##STR163## uniformly dyes polyester/cotton mixed fabric, from weaklyacid solutions by the processes of Examples 2 and 3, in blue shadeswhich are fast to light, wet processing and rubbing.

A similar dyestuff is obtained if, instead of the1-amino-3-dimethylaminopropane, an equivalent amount of1-amino-3-methylaminopropane is employed.

EXAMPLE 133

15 g of the intermediate product of the formula ##STR164## obtainedaccording to Example 6, are suspended in 100 ml of toluene at 20°. 6.2 gof N-2-hydroxyethylpiperazine in 20 ml of toluene are added dropwise inthe course of 30 minutes and the mixture is subsequently stirred for afurther 30 minutes. The dyestuff which has precipitated is filtered off,washed with 100 ml of toluene and then with petroleum ether and dried at50° in a circulating air cabinet. The resulting dyestuff corresponds tothe formula ##STR165## and uniformly dyes polyester/cotton mixtures, bythe processes of Examples 2 and 3, in red shades which are very fast towet processing.

A similar dyestuff is obtained if 4.3 parts of N-methylpiperazine areemployed instead of the N-2-hydroxyethylpiperazine.

EXAMPLE 134

19.2 g of 1-amino-4-(3-dimethylamino-1-propylamino)-anthraquinone(prepared by reacting 1-amino-4-bromoanthraquinone-2-sulphonic acid with1-amino-3-dimethylaminopropane and then eliminating the sulphonic acidgroup by reduction) are introduced into 150 ml of toluene and 15 ml ofdimethylformamide. 5.6 g of 2,4,6-trifluorotriazine are added dropwiseto the mixture in the course of 5 minutes. During this addition, thetemperature may rise to 30°-35°. The mixture is subsequently stirred for30 minutes in order to bring the condensation reaction to completion.11.4 g of phenol are now introduced into the reaction mixture, and 9.1 gof triethylamine are added dropwise. The temperature is then kept at30°-35° for 30 minutes and at 50° for a further 30 minutes. When thereaction has ended, the mixture is cooled to 20°, the dyestuff which hasprecipitated is filtered off and the filter cake is washed with tolueneand dried at 60° in a circulating air cabinet. The resulting dyestuff ofthe formula ##STR166## is soluble in dilute acetic acid and dyespolyester/cotton mixtures, in a very uniform manner by the processes ofExamples 2 and 3, in blue shades which are fast to wet processing andrubbing.

Further dyestuffs, listed in Table VI, which uniformly dyepolyester/cotton mixtures in the colour shades indicated from an aceticacid solution by the processes of Examples 2 and 3 can be preparedanalogously.

                                      TABLE VI    __________________________________________________________________________    Example    No.    Dyestuff                                       Colour    __________________________________________________________________________                                                          shade    135            ##STR167##                                    red    136            ##STR168##                                    blue    137            ##STR169##                                    blue    138            ##STR170##                                    blue    139            ##STR171##                                    blue    140            ##STR172##                                    blue    141            ##STR173##                                    blue    142            ##STR174##                                    green    __________________________________________________________________________

EXAMPLE 143

19.2 g of 1-amino-4-(3-dimethylamino-1-propylamino)-anthraquinone arereacted with 5.6 g of 2,4,6-trifluorotriazine as in Example 134.

12.4 g of 1-amino-3-dimethylaminopropane are added dropwise to thesuspension of the resulting difluorotriazinylaminoanthraquinone in thecourse of 20 minutes. During this addition, the temperature may rise to30°-35°. The mixture is then subsequently stirred for one hour, afterwhich the reaction has ended. The precipitate is filtered off, washedwith toluene and dried at 60° in a circulating air cabinet. Theresulting dyestuff corresponds to the formula ##STR175## and uniformlydyes polyester/cotton mixed fabric, from an acetic acid solution by theprocesses of Examples 2 and 3, in blue shades which are fast to wetprocessing and rubbing.

EXAMPLE 144

5 g of bleached pulp are dispersed in 200 ml of water. A solution of0.05 g of the dyestuff of Example 6 in 2 ml of 5% strength acetic acidis added and the mixture is stirred at 20° for some minutes and dilutedwith 500 ml of water. 10 ml of a 1% strength resin size solution and 15ml of a 1% strength aluminium sulphate solution are then added. Theresulting suspension is subsequently stirred for 15 minutes. Thecoloured mass is filtered on a sheet-forming unit. After drying, abluish-tinged red-coloured sheet of paper is obtained.

EXAMPLE 145

17.0 g of 4-methylamino-2'-hydroxy-5'-methylazobenzene are suspended ordissolved in 80 ml of toluene and 9.8 g of N,N-dimethylaniline. 10.5 gof 2,4,6-trifluorotriazine are added dropwise at 20° in the course of 10minutes and the mixture is subsequently stirred for 45 minutes. When thecondensation reaction has ended, 14.2 g of N-methylpiperazine are addeddropwise in the course of 30 minutes, the resulting suspension issubsequently stirred at 35°-40° for 2 hours and the dyestuff which hasprecipitated is filtered off at 20°, washed with toluene and dried at60° in a circulating air cabinet. The product corresponds to the formula##STR176## and gives, on polyester/cotton mixtures from an acetic acidsolution by the processes of Examples 2 and 3, solid strong yellowdyeings with good fastness to light, wet processing and rubbing.

The dyestuff produces strong yellow dyeings on paper by the process ofExample 144.

EXAMPLES 146-153 The following basic fluorotriazine-azo dyestuffs, whichgive, on polyester/cotton mixtures by the processes of Examples 2 and 3,dyeings which are likewise fast to light, wet processing and rubbing,can also be obtained by the same procedures as described in Examples74-76.

    __________________________________________________________________________    Ex-    ample    No. Dyestuff                                            Colour    __________________________________________________________________________                                                            shade    146         ##STR177##                                         yellow    147         ##STR178##                                         yellow    148         ##STR179##                                         yellow    149         ##STR180##                                         red    150         ##STR181##                                         red    151         ##STR182##                                         blue    152         ##STR183##                                         blue    153         ##STR184##                                         orange-red    __________________________________________________________________________

We claim:
 1. Process for dyeing and printing fibre blends of celluloseand synthetic fibres characterized in that a reactive dyestuff which isfree from anionic groups and which contains a basic group and ahalogenotriazinyl radical, such dyestuff having the formula ##STR185##in which D is the radical of an organic azo dyestuff which is free fromanionic groups and is free from basic groups,B is a direct bond to aring carbon atom of D, R₁ is H, alkyl, aralkyl or aryl and W is afluorotriazinyl radical containing a basic group of one of the followingformulae ##STR186## in which V is ##STR187## or a direct bond, B₁ is abridge member selected from the group consisting of C₂ -C₈ -alkylene,aralkylene, aralkylalkylene and alkarylene or, if ##STR188## also adirect bond, R₂, R₃, and R₄ and R₅ are H or alkyl and R₂ and R₅ maytogether represent alkylene, P1 An .sup.⊖ is an anion and HX is anorganic or inorganic acid,is used in a single stage process in weaklyacidic medium.
 2. Process of claim 1 wherein the reactive dyestuffcontains a bridge member wherein B₁ is C₂ -C₈ -alkarylene oralkarylalkylene, or if V=NR₅ also a direct bond.
 3. Process of claim 1wherein the reactive dyestuff is one in whichW is a fluorotriazinylradical containing a basic group of one of the following formulae:##STR189## in which B₂ denotes a direct bond, phenylene or phenylene-O-and alkylene denotes C₂ -C₈ -alkylene.
 4. Process of claim 1 wherein thereactive dyestuff is one in whichW is a fluorotriazinyl radicalcontaining a basic group of one of the following formulae ##STR190##wherein alkyl denotes C₁ -C₄ -alkyl which is optionally substituted byOH.